The Immune Response Enhanced by Beta-1,3D Glucan - pg.2

The Immune Response Enhanced by Beta-1,3D Glucan by A.J.Lanigan - pg.2

As part of the continuing process, IL-1 helps activate B and T cells; IL-2 instructs other helper T's and a different class of T cells, the killer T's (CTLs or cytotoxic T lymphocytes), to multiply. The proliferating helper T's in turn release substances that cause B cells to multiply and produce antibodies. B cells are prepared to recognize antigen without preprocessing. The T cell cannot recognize antigen in its natural state. It must first be broken down and the fragments bound to a Major Histocompatibility Complex (MHC) molecule by the APC. The macrophage is an APC. Glucan causes its receptor sites (key slots) to be released for these presentation chores.

The killer T cells (trained assassins) now begin shooting holes in cells that have been infected by viruses or other pathogens. The killer T cell (CTL or cytotoxic T lymphocyte) becomes a "trained assassin". They respond to the MHC I complex, which is found on almost all body cells. The CTL has the ability to seek and destroy infected human cells in a specific manner. With the injection of powerful chemicals, these infected cells are killed before they can be used to spread a disease. Natural Killer (NK) cells are large, granule-filled lymphocytes that take on tumor cells and infected body cells. They are known as "natural" killers because they attack without first having to recognize specific antigens. Like the macrophage, if it is not "self", it will proceed to kill. NK cells and CTLs both kill on contact. The killer binds to the target, aims its weapons and then releases a lethal burst of chemicals to punch holes in the target. - source

The Immune Response Enhanced by Beta-1,3D Glucan - pg.3

The Immune Response Enhanced by Beta-1,3D Glucan by A.J.Lanigan - pg.3

When a Class II MHC molecule is presented by the APC, the B cell/antibody process begins. This is the humoral side of the immune system. The antibodies released by the B cells bind to antigens on the surfaces of free-floating viruses. Besides making it easier for macrophages to destroy viruses, this binding signals blood components called complement to puncture holes in the viruses. The Complement System is made up of 25 proteins that work with the antibodies to destroy invaders. They facilitate phagocytosis (eating by phagocytes) or they directly puncture the invader's cell membrane. C3 is the key protein that triggers the "complement cascade". This cascade results into a "membrane attack complex" that literally blasts a hole into the antibody marked prey. Fragments thrown off by this process bring into play mast cells and basophils. By releasing their chemical contents, they produce the rediness, warmth, and swelling of the inflammatory response.

Finally, as the infection is brought under control, the activated T and B cells are turned off by suppressor T cells (a T-8 subset). However, a few "memory cells" (another T-8 subset) remain behind to respond quickly if the same virus attacks again. Immunologists believe that the body fights cancer in much the same way it seeks to eliminate viruses. Further study of the immune system is expected to reveal ways to bolster it, allowing the body to become a more active partner in the fight against cancer. - source